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Fig. 6 | Molecular Cytogenetics

Fig. 6

From: 7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype

Fig. 6

Genome Browser image comparing HFGS cases by microdeletion, included in Table 1. The red rectangle demarcates the minimum region (including the HOXA cluster) proposed as responsible for the phenotype of these patients. The most important genes that correlate with the proposed phenotype are: the HOXA13 gene (gray circle), the HOXA1 and HOXA2 genes (blue circle), the HOXA5 and HOXA11 genes (orange circle), and miRNA196b (green circle)

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